Jan Demol is a highly experienced professional in regulatory affairs and biosafety, currently serving as Regulatory Affairs Manager and Biosafety Manager at Materialise since March 2016. In these roles, responsibilities include ensuring compliance with biocompatibility, cleaning, sterilization, and packaging standards for personalized medical devices, conducting biosafety evaluations, and liaising with regulatory agencies. Previously, Jan held the position of Regulatory Project Manager at Mobelife from December 2011 to February 2016, where roles included Quality Manager and R&D Project Manager. Jan's academic background includes a PhD in Engineering Sciences and a Master of Science in Mechanical Engineering, both obtained from KU Leuven. The PhD focused on the in vitro and in silico analysis of fibrin for bone engineering applications.
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